Alkanethioimidoyl Radicals: Evaluation of β-Scission Rates and of Cyclization onto S-Alkenyl Substituents-Reference-Cited by-同舟云学术

Alkanethioimidoyl Radicals: Evaluation of β-Scission Rates and of Cyclization onto S-Alkenyl Substituents

Published:2004-02-19 Issue:6 Volume:69 Page:2056-2069
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Minozzi Matteo¹,Nanni Daniele¹,Walton John C.¹

Affiliation:

1. School of Chemistry, University of St. Andrews, Fife, KY16 9ST, United Kingdom, and Dipartimento di Chimica Organica “A. Mangini”, Università di Bologna, Viale Risorgimento 4, I-40136 Bologna, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0353637

Reference53 articles.

1. Aromatic annelation by reaction of arylimidoyl radicals with alkynes: a new synthesis of quinolines

2. Aromatic annelation by reaction of arylimidoyl radicals with alkynes: evidence for the intervention of a spirocyclohexadienyl radical in the synthesis of substituted quinolines

3. 4 + 1 Radical annulations with isonitriles: a simple route to cyclopenta-fused quinolines

4. Tandem Radical Reactions of Carbon Monoxide, Isonitriles, and Other Reagent Equivalents of the Geminal Radical Acceptor/Radical Precursor Synthon

5. A General Synthetic Approach to the (20S)-Camptothecin Family of Antitumor Agents by a Regiocontrolled Cascade Radical Cyclization of Aryl Isonitriles

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